Canonical Allele Identifier: CA414755768
Gene: CD40LG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659137T>C , CM000685.2:g.136659137T>C GRCh38
NC_000023.10:g.135741296T>C , CM000685.1:g.135741296T>C GRCh37
NC_000023.9:g.135568962T>C NCBI36
NG_007280.1:g.15961T>C , LRG_141:g.15961T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*126T>C ENSP00000512122.1:n.*126T>C
ENST00000695725.1:c.*63T>C ENSP00000512123.1:n.*63T>C
ENST00000695726.1:n.2476T>C
ENST00000695729.1:n.3311T>C
ENST00000370629.7:c.508T>C MANE Select ENSP00000359663.2:p.Tyr170His
ENST00000370628.2:c.445T>C ENSP00000359662.2:p.Tyr149His
ENST00000370629.6:c.508T>C ENSP00000359663.2:p.Tyr170His
NM_000074.2:c.508T>C , LRG_141t1:c.508T>C NP_000065.1:p.Tyr170His
NM_000074.3:c.508T>C MANE Select NP_000065.1:p.Tyr170His